位阻效应
材料科学
三元运算
富勒烯
有机太阳能电池
结晶度
分子
侧链
能量转换效率
相(物质)
化学工程
有机化学
光电子学
聚合物
化学
复合材料
程序设计语言
工程类
计算机科学
作者
Yuan Chang,Jianquan Zhang,Yuzhong Chen,Gaoda Chai,Xiaopeng Xu,Liyang Yu,Ruijie Ma,Yu Han,Tao Liu,Pei Liu,Qiang Peng,He Yan
标识
DOI:10.1002/aenm.202100079
摘要
Abstract In this work, the properties and performance of three structurally similar non‐fullerene acceptors (named BTP‐Ph, BTP‐Th, and BTP‐C11) possessing different side chains on the β‐positions of the thienothiophene units of the Y6 molecule are systematically studied. The steric and electronic effects of these side chains on the blend morphology and device performance based on the PTQ10 donor polymer are investigated. It is found that the thiophene and benzene units on the side chains introduce more steric hindrance and thus slightly reduce the crystallinity of the molecule. However, an interesting matching trend with the PTQ10 donor that appears to better match with the less crystalline molecules is observed. Overall, PTQ10:BTP‐Ph delivers the highest performance of 17.1% due to the suitable phase separation among three blends. Next, a ternary strategy is explored by incorporating BTP‐Th/BTP‐C11 with better molecular packing into PTQ10:BTP‐Ph, which successfully extends photon response, enhances charge transport, and suppresses charge recombination compared with the binary blend. Due to these synergistic effects, the ternary device based on PTQ10:BTP‐Ph:BTP‐Th achieves an outstanding power conversion efficiency of 17.6% with a fill factor of 78.8%, which is the highest value of PTQ10‐based devices to date.
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